A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149328



Internal ID15529411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83994518..84005144hg38UCSC Ensembl
Innerchr16:84028123..84038749hg19UCSC Ensembl
Innerchr16:82585624..82596250hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3810627
hg1910627
hg1810627
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573414
Supporting Variants
SamplesHGDP00784
Known GenesNECAB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149328
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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